EN ISO 24998:2008
Current
The latest, up-to-date edition.
Plastics laboratory ware - Single-use Petri dishes for microbiological procedures (ISO 24998:2008)
11-15-2008
Foreword
1 Scope
2 Terms and definitions
3 Principle of use
4 Types
5 Material
6 Design and construction
6.1 General
6.2 Dimensions
6.3 Rim on lid
6.4 Compartments
6.5 Venting
7 Performance
7.1 Rigidity
7.2 Resistance to thermal distortion
7.3 Resistance to fracture
7.4 Stability in stacking
8 Limitation of contamination
9 Sterility and special microbiological states
10 Packaging
11 Marking
Annex A (normative) Type test for rigidity
Annex B (normative) Type test for resistance to thermal
distortion
Annex C (normative) Type test for resistance to fracture
Annex D (normative) Type test for stability in stacking
Bibliography
ISO 24998:2008 specifies requirements and test methods for plain, single-use Petri dishes for microbiological use.ISO 24998:2008 does not apply to products of similar design which may be used for cell or tissue culture purposes. Neither does it apply to dishes supplied ready loaded with microbiological media.
| Committee |
CEN/TC 332
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Current
|
| Standards | Relationship |
| DIN EN ISO 24998:2009-03 | Identical |
| NS EN ISO 24998 : 1ED 2008 | Identical |
| UNE-EN ISO 24998:2009 | Identical |
| PN EN ISO 24998 : 2009 | Identical |
| NEN EN ISO 24998 : 2008 | Identical |
| ISO 24998:2008 | Identical |
| BS EN ISO 24998:2008 | Identical |
| NBN EN ISO 24998 : 2009 | Identical |
| NF EN ISO 24998 : 2009 | Identical |
| SN EN ISO 24998:2009 | Identical |
| I.S. EN ISO 24998:2008 | Identical |
| UNI EN ISO 24998 : 2009 | Identical |
| ISO 11137-1:2006 | Sterilization of health care products Radiation Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices |
| ISO 14644-6:2007 | Cleanrooms and associated controlled environments Part 6: Vocabulary |
| ISO 14644-8:2013 | Cleanrooms and associated controlled environments Part 8: Classification of air cleanliness by chemical concentration (ACC) |
| ISO 14644-2:2015 | Cleanrooms and associated controlled environments Part 2: Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration |
| ISO 14644-5:2004 | Cleanrooms and associated controlled environments — Part 5: Operations |
| ISO 14644-3:2005 | Cleanrooms and associated controlled environments Part 3: Test methods |
| ISO 14644-7:2004 | Cleanrooms and associated controlled environments — Part 7: Separative devices (clean air hoods, gloveboxes, isolators and mini-environments) |
| ISO 14644-1:2015 | Cleanrooms and associated controlled environments Part 1: Classification of air cleanliness by particle concentration |
| ISO 14644-4:2001 | Cleanrooms and associated controlled environments — Part 4: Design, construction and start-up |
| ISO 17665-1:2006 | Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices |
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